Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants.
Clin Genet
; 92(2): 224-226, 2017 08.
Article
in En
| MEDLINE
| ID: mdl-28044327
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ataxia
/
Ubiquinone
/
Muscle Weakness
/
Mitochondrial Diseases
/
Mutation
/
Nephrotic Syndrome
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Clin Genet
Year:
2017
Document type:
Article
Affiliation country: